The transcription factor Sox10 is a key regulator of peripheral glial development

Stefan Britsch, Derk E. Goerich, Dieter Riethmacher, +5

Genes & Development

Sensory Nerves Determine the Pattern of Arterial Differentiation and Blood Vessel Branching in the Skin

Yoh‐suke Mukouyama, Donghun Shin, Stefan Britsch, +2

Cell

Peripheral NerveAnatomyDermatologyPeripheral NervesBlood Vessel Branching +15

Conditional mutation of the ErbB2 (HER2) receptor in cardiomyocytes leads to dilated cardiomyopathy

C. Özcelik, Bettina Erdmann, Bernhard Pilz, +6

Proceedings of the National Academy of Sciences

The ErbB2 and ErbB3 receptors and their ligand, neuregulin-1, are essential for development of the sympathetic nervous system

Stefan Britsch, Li Li, Susanne Kirchhoff, +4

Genes & Development

Neural Crest CellsNeurotransmitterPeripheral Nervous SystemErbb3 ReceptorsSympathetic Nervous System +16

Peripheral nervous system defects in erbB2 mutants following genetic rescue of heart development

M. T. Woldeyesus, Stefan Britsch, Dieter Riethmacher, +6

Genes & Development

The Neuregulin-I/ErbB Signaling System in Development and Disease

Stefan Britsch

Advances in anatomy, embryology and cell biology

Signal TransductionNeuregulin-i/erbb Signaling SystemDevelopmental BiologySignaling PathwayDisease Mechanism +3

Novel p62dok family members, dok-4 and dok-5, are substrates of the c-Ret receptor tyrosine kinase and mediate neuronal differentiation

Jan Grimm, Martin M. Sachs, Stefan Britsch, +4

The Journal of Cell Biology

Family MembersCellular NeurobiologySynaptic SignalingSignaling PathwayCell Regulation +16

The bHLH factor Olig3 coordinates the specification of dorsal neurons in the spinal cord

Thomas Müller, Katrin Anlag, Hendrik Wildner, +3

Genes & Development

Dorsal Spinal CordGeneticsPeripheral NervesCellular NeurobiologyPeripheral Nervous System +18

A role of the cryptic gene in the correct establishment of the left–right axis

Ursula Gaio, Axel Schweickert, Anja Fischer, +8

Current Biology

Developmental BiologyDevelopmental GeneticsGeneticsGene StructureGenetic Mechanism +9

BCL11B mutations in patients affected by a neurodevelopmental disorder with reduced type 2 innate lymphoid cells

Davor Lessel, Christina Gehbauer, Nuria C. Bramswig, +45

Brain

Bcl11b MutationsBrain DevelopmentLymphocyte DevelopmentGeneticsInnate Lymphoid Cells +19